A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952536



Internal ID17301410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:32031664..32051063hg38UCSC Ensembl
Outerchr13:32605801..32625200hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg3819400
hg1919400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998205
SamplesBILGI_BIOE
Known GenesFRY
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952536
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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